Search results for " monitoring" in Resources
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				FDA’s Adverse Event Reporting System (AERS)
								
	The Adverse Event Reporting System (AERS) is a computerized information database designed to support the FDA's post-marketing safety surveillance program for all approved drug and therapeutic biolog…								
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				World Health Organization
								…standards, articulating evidence-based policy options, providing technical support to countries, and monitoring and assessing health trends.